D. Hale

发表

Fatty acid oxidation disorders: a new class of metabolic diseases.

D. Hale, M. Bennett, M. Bennett, 1992, The Journal of pediatrics.

Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chainl-3-hydroxyacyl-CoA dehydrogenase deficiency

P. Kaplan, M. Bennett, G. Berry, 1993, Journal of Inherited Metabolic Disease.

Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency.

D. Dawson, M. Bennett, L. Waber, 1995, The Journal of pediatrics.

Ca2+ responses to interleukin 1 and tumor necrosis factor in cultured human skin fibroblasts. Possible implications for Reye syndrome.

J. Deeney, B. Corkey, S. Douglas, 1991, The Journal of clinical investigation.

Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiency.

A. Bhala, M. Bennett, D. Hale, 1993, The Journal of pediatrics.

Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

E. Bertini, F. Zacchello, C. Bachmann, 1991, The Journal of pediatrics.

Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency.

R. Kelley, D. Hale, B. Taubman, 1987, Pediatrics.

Short‐chain L‐3‐hydroxyacyl‐CoA dehydrogenase deficiency in muscle: A new cause for recurrent myoglobinuria and encephalopathy

S. Dimauro, N. York, I. Tein, 1991, Annals of neurology.

Identification of urinary metabolites of (+/-)-2-(p-isobutylphenyl)propionic acid (Ibuprofen) by routine organic acid screening.

A. Bhala, M. Bennett, D. Hale, 1992, Clinica chimica acta; international journal of clinical chemistry.

Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder

M. Bennett, J. Vamecq, R. Pollitt, 1991, Journal of Inherited Metabolic Disease.

PRENATAL DIAGNOSIS OF MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY IN FAMILY WITH SUDDEN INFANT DEATH

P. Coates, N. Manning, M. Bennett, 1987, The Lancet.

A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts.

E. Bertini, D. Hale, K. Gibson, 1994, The Journal of pediatrics.

Progress in Reye syndrome: epidemiology, biochemical mechanisms and animal models.

S. Douglas, D. Hale, L. Kilpatrick-Smith, 1989, Digestive diseases.

Azelaic and pimelic acids: Metabolic intermediates or artefacts?

M. Bennett, M. Ragni, D. Hale, 1992, Journal of Inherited Metabolic Disease.